Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02080 | A10 | 979411 | C | T | missense_variant | MODERATE | c.886G>A|p.Asp296Asn |
S150 |
2 | BAA10g02080 | A10 | 979730 | C | T | synonymous_variant | LOW | c.567G>A|p.Arg189Arg |
S269 |
3 | BAA10g02080 | A10 | 979762 | C | T | missense_variant | MODERATE | c.535G>A|p.Glu179Lys |
S11 S233 |
4 | BAA10g02080 | A10 | 979876 | C | T | missense_variant | MODERATE | c.421G>A|p.Val141Ile |
S152 |
5 | BAA10g02080 | A10 | 982676 | C | T | upstream_gene_variant | MODIFIER | c.-2380G>A| |
S188 |
6 | BAA10g02080 | A10 | 983532 | G | A | upstream_gene_variant | MODIFIER | c.-3236C>T| |
S50 |